T

Terrestrial Bio

Makes silk skin patches for needle-free vaccines

QC Analyst / Research Associate - Chromatography Focus

Regulatory & Quality (Life Sciences)Updated on Nov 9
Full-time$60k - $75k

About the Job

Requirements

  • A bachelor's degree in Chemistry, Biochemistry, Chemical Engineering, or a related field with 1–3 years of experience, or a master's degree with relevant laboratory experience.
  • Hands-on experience operating HPLC/UPLC systems; Agilent systems and OpenLab CDS experience are strongly preferred.
  • Practical experience with chromatographic techniques including reverse-phase, SEC, and IEX.
  • Experience supporting QC release or stability testing in a GMP-aligned or GLP environment.
  • Strong attention to detail and ability to follow SOPs precisely.
  • Excellent documentation practices and understanding of data integrity.
  • Strong organizational skills with the ability to manage multiple workflows and prioritize effectively in a fast-paced environment.
  • Excellent verbal and written communication skills and comfort working within interdisciplinary teams.

Responsibilities

  • Perform routine QC in-process, release, and stability testing using HPLC/UPLC methods including reverse-phase, SEC, and IEX.
  • Perform HPLC/UPLC method development and troubleshooting in collaboration with senior scientists to support the QC workflow.
  • Prepare samples, operate Agilent systems, verify system suitability, and ensure analyses meet method and specification requirements.
  • Execute complementary analytical assays such as UV-Vis, pH, surface tension, and mechanical tests.
  • Maintain complete, accurate documentation in compliance with cGMP, ALCOA+, and data integrity requirements.
  • Conduct routine instrument care, including solvent flushes, column care, and daily checks.
  • Process and review chromatographic data in Agilent OpenLab CDS.
  • Support method qualification, validation, and transfer activities by executing protocols and recording observations.
  • Maintain calibration, maintenance, and service records for analytical instrumentation.
  • Write and maintain key technical documentation including SOPs, analytical protocols, technical reports, and audit-ready records; contribute to regulatory submissions.
  • Collaborate cross-functionally with QC, Analytical Development, Process Development, Manufacturing, and Regulatory teams to enable program success.

Desired Qualifications

  • Agilent systems and OpenLab CDS experience.

About the Company

Terrestrial Bio

Makes silk skin patches for needle-free vaccines

Terrestrial Bio develops silk-based patches that deliver vaccines and therapies through the skin, using dissolvable silk tips to release the dose over time for needle-free delivery. A patch is applied to the skin and the silk components dissolve in a controlled sequence to dispense the medication at the right dose, with release spanning minutes to months. This approach differs from traditional injections by providing a self-administered, long-lasting, painless delivery method and emphasizing partnerships with healthcare providers and pharmaceutical groups. The goal is to improve global health by offering effective, easy-to-use, shelf-stable vaccines and therapies at scale through collaborations.

Company size
51-200
Company stage
Grant
Total funding
$162.1M
Headquarters
Cambridge, MA
Founded
2012

Recently Posted Jobs

Explore more opportunities at Terrestrial Bio

See more jobs